Canonical Allele Identifier: CA2237032107
Gene: GAN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.81354378_81354383delinsTATAAG , CM000678.2:g.81354378_81354383delinsTATAAG GRCh38
NC_000016.9:g.81387983_81387988delinsTATAAG , CM000678.1:g.81387983_81387988delinsTATAAG GRCh37
NC_000016.8:g.79945484_79945489delinsTATAAG NCBI36
NG_009007.1:g.44413_44418delinsTATAAG , LRG_242:g.44413_44418delinsTATAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000648349.2:c.168-27_168-22delinsTATAAG ENSP00000498114.1:n.168-27_168-22delinsTATAAG
ENST00000648994.2:c.283-27_283-22delinsTATAAG MANE Select ENSP00000497351.1:n.283-27_283-22delinsTATAAG
ENST00000650388.1:c.168-2407_168-2402delinsTATAAG ENSP00000498081.1:n.168-2407_168-2402delinsTATAAG
ENST00000674788.1:n.408-27_408-22delinsTATAAG
ENST00000568107.2:c.283-27_283-22delinsTATAAG ENSP00000476795.1:n.283-27_283-22delinsTATAAG
NM_022041.3:c.283-27_283-22delinsTATAAG , LRG_242t1:c.283-27_283-22delinsTATAAG NP_071324.1:n.283-27_283-22delinsTATAAG
XM_017023734.1:c.-357-27_-357-22delinsTATAAG XP_016879223.1:n.-357-27_-357-22delinsTATAAG
NM_001377486.1:c.-357-27_-357-22delinsTATAAG NP_001364415.1:n.-357-27_-357-22delinsTATAAG
NM_022041.4:c.283-27_283-22delinsTATAAG MANE Select NP_071324.1:n.283-27_283-22delinsTATAAG